Literature DB >> 12960512

The production of tumor necrosis factor-alpha by macrophages in rats with acute alcohol loading.

Toshiyuki Kitazawa1, Yoshihiro Nakatani, Masao Fujimoto, Nobuhiro Tamura, Masahito Uemura, Hiroshi Fukui.   

Abstract

BACKGROUND: It is suggested that endotoxin, proinflammatory cytokines, and lipopolysaccharide-binding protein (LBP) play an important role in the development of alcoholic liver disease. Our previous study showed that splenic macrophages were important for endotoxin uptake and excessive production of tumor necrosis factor (TNF) in rats given large amounts of alcohol. To study the pathophysiological roles of macrophages in alcoholic liver diseases, we examined the production of TNF-alpha by rat Kupffer cells, splenic macrophages, and alveolar macrophages with acute alcohol loading in the presence or absence of LBP.
METHODS: Kupffer cells, splenic macrophages, and alveolar macrophages were isolated from male Wistar rats given 5 mg/g body weight of ethanol intraperitoneally after an hour. The production of TNF-alpha by these cells incubated with endotoxin 100 ng/ml in the presence or absence of LBP (1% rat serum) was determined.
RESULTS: Acute alcohol loading did not affect the production of TNF-alpha by Kupffer cells. With acute alcohol loading, splenic macrophages tended to produce more TNF-alpha. Alveolar macrophages produced more TNF-alpha than Kupffer cells, and although the production of TNF-alpha by alveolar macrophages tended to be suppressed by acute alcohol loading, the production of TNF-alpha by alveolar macrophages still remained high in the presence of rat serum.
CONCLUSIONS: Splenic macrophages and alveolar macrophages may be related to excessive production of TNF-alpha in acute alcoholics with endotoxemia.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12960512     DOI: 10.1097/01.ALC.0000078611.55696.F0

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  6 in total

1.  Perturbation of chemokine networks by gene deletion alters the reinforcing actions of ethanol.

Authors:  Yuri A Blednov; Susan E Bergeson; Danielle Walker; Vania M M Ferreira; William A Kuziel; R Adron Harris
Journal:  Behav Brain Res       Date:  2005-08-18       Impact factor: 3.332

2.  Alcohol Consumption Accumulation of Monocyte Derived Macrophages in Female Mice Liver Is Interferon Alpha Receptor Dependent.

Authors:  Khaled Alharshawi; Holger Fey; Alyx Vogle; Tori Klenk; Miran Kim; Costica Aloman
Journal:  Front Immunol       Date:  2021-04-30       Impact factor: 7.561

Review 3.  The effect of inflammatory cytokines in alcoholic liver disease.

Authors:  Hideto Kawaratani; Tatsuhiro Tsujimoto; Akitoshi Douhara; Hiroaki Takaya; Kei Moriya; Tadashi Namisaki; Ryuichi Noguchi; Hitoshi Yoshiji; Masao Fujimoto; Hiroshi Fukui
Journal:  Mediators Inflamm       Date:  2013-12-09       Impact factor: 4.711

4.  Ginsenoside Rb1 Alleviates Alcohol-Induced Liver Injury by Inhibiting Steatosis, Oxidative Stress, and Inflammation.

Authors:  Yuqi Lai; Qinxiang Tan; Shu Xv; Sha Huang; Yuhua Wang; Yunjia Li; Ting Zeng; Chan Mo; Yuyao Chen; Shaohui Huang; Chuying Zhou; Lei Gao; Zhiping Lv
Journal:  Front Pharmacol       Date:  2021-02-26       Impact factor: 5.810

5.  Protective and therapeutic effects of an extract mixture of alder tree, labiate herb, milk thistle green bean-rice bran fermentation, and turnip against ethanol-induced toxicity in the rat.

Authors:  Min-Won Baek; Seung-Hyeok Seok; Hui-Young Lee; Dong Jae Kim; Byoung-Hee Lee; Young-Tae Ahn; Kwang-Sei Lim; Chul-Sung Huh; Jae-Hak Park
Journal:  J Vet Sci       Date:  2008-03       Impact factor: 1.672

6.  Inhibitory Effect of Gardenoside on Free Fatty Acid-Induced Steatosis in HepG2 Hepatocytes.

Authors:  Huiqing Liang; Limin Zhang; Hongguo Wang; Jinmo Tang; Jiaen Yang; Chuncheng Wu; Shaodong Chen
Journal:  Int J Mol Sci       Date:  2015-11-20       Impact factor: 5.923

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.